• Merck & Co. (Rahway, NJ)
    …trace impurity quantitation (eg, carcinogens/mutagens such as nitrosamines).Utilize specialized instrumentation such as mass spectrometers and other spectroscopic ... techniques.Collaborate closely with internal company sites and Contract Manufacturing Organizations (CMOs) within the manufacturing network to:Identify issues… more
    HireLifeScience (07/31/25)
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  • Tris Pharma (Monmouth Junction, NJ)
    …according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs) procedures. The incumbent prepares, coordinates and advances ... for assigned projects regularly reporting status/issues to management, conducts laboratory investigations and recommends appropriate Corrective Action Preventive Action… more
    HireLifeScience (07/30/25)
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  • cGMP Manufacturing

    University of Southern California (Los Angeles, CA)
    cGMP Manufacturing Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA ... Health-Sciences-Campus/ cGMP - Manufacturing - Specialized - Laboratory -Technician\_REQ20160209/apply) Keck School of Medicine Los Angeles, California The… more
    University of Southern California (06/11/25)
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  • cGMP Quality Control (QC)…

    University of Southern California (Los Angeles, CA)
    … Quality Control (QC) Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ ... Manufacturing Practices ( cGMP ) facility. The cGMP Quality Control (QC) Specialized Lab Technician...test results, etc.) + Trains investigators and students in specialized laboratory techniques. Provides technical consulting in… more
    University of Southern California (06/09/25)
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  • cGMP Process Development (PD) Specialist

    University of Southern California (Los Angeles, CA)
    …and assay development, assay qualification, support tech transfer of processes) from cGMP manufacturing and assays to quality control. Develops and reviews ... it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a...GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work… more
    University of Southern California (06/09/25)
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  • Sr cGMP Specialist - QC Analytical…

    Houston Methodist (Houston, TX)
    …with core users to assist in the translation of research processes to the cGMP manufacturing facility. + Seeks opportunities to expand learning beyond baseline ... years of biotechnology or pharmaceutical industry experience with exposure to cGMP manufacturing operations + Experience performing equipment validation… more
    Houston Methodist (07/30/25)
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  • cGMP Senior Quality Control (QC) Specialist

    University of Southern California (Los Angeles, CA)
    …Practices (eg, cGMPs, GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work as an individual ... cGMP Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP more
    University of Southern California (07/30/25)
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  • Laboratory Technician

    Actalent (Decatur, IL)
    …in monthly safety audits and complete safety engagements. + Follow Good Manufacturing Practices ( cGMP ) and regulatory guidelines. + Collaborate with team ... + Experience in a regulated environment with knowledge of cGMP , FDA, or other regulatory standards. + Long-term job...position is based in a professional Quality Control (QC) laboratory within a manufacturing facility. The culture… more
    Actalent (07/24/25)
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  • Microbiology Laboratory Technician

    Actalent (Norcross, GA)
    …microbial growth on plates and perform isolation plating. + Adhere to cGMP (current Good Manufacturing Practices) and other regulatory requirements applicable ... Actively Interviewing for Lab Technologist - Microbiology to join top medical laboratory in Norcross, GA! Description + Competently perform all assigned departmental… more
    Actalent (07/26/25)
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  • Blood & Tissue Manufacturing Associate…

    BioBridge Global (San Antonio, TX)
    …all Standard Operating Procedures (SOPs), organizational policies, and regulatory and cGMP /cGTP requirements. Will prepare specialized blood components and ... tissue recovery from living and deceased donors._ Job Title: Blood & Tissue Manufacturing Associate I Revision: 0002 Job Code: 700236 Shift: Saturday, Sunday and… more
    BioBridge Global (07/28/25)
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  • Blood & Tissue Manufacturing Technician I,…

    BioBridge Global (San Antonio, TX)
    manufacturing , final labeling, and quarantine procedures. Ensures all laboratory procedures and processes are conducted in compliance with prescribed ... Requires an Associate Degree from an accredited college or university in a specialized area. The required major is Clinical Laboratory Science or equivalent.… more
    BioBridge Global (07/08/25)
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  • Chemical Process Technician

    Cambrex High Point (Waltham, MA)
    …equipment use and care logs + Work with scientists and engineers to execute manufacturing activities according to cGMP regulations at the highest quality + ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow,...+ Minimum of 1 year of chemical or biotech manufacturing experience, in particular under cGMP . +… more
    Cambrex High Point (06/21/25)
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  • Sanitation Specialist

    ADM (Kennesaw, GA)
    …Sanitation Specialist - Kennesaw, GA **Department/Function:** Operations: Manufacturing , Production, Maintenance, Utilities **Job Description:** Job Description: ... and grounds as needed in order to maintain and conform to FDA and cGMP guidelines and regulations for cleaning practices. GMP training and training on specialized more
    ADM (07/22/25)
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  • QC Data Review

    Cambrex High Point (Charles City, IA)
    …to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing ... from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (06/05/25)
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  • Quality Assurance Associates I Or II - Open Pool

    Colorado State University (Fort Collins, CO)
    …is responsible for the implementation and execution of policies and procedures for the cGMP manufacturing of biologics. Individuals will be working within a ... outdoor opportunities. CSU BioMARC is a nonprofit contract development and manufacturing organization focused on the production of biopharmaceutical materials for… more
    Colorado State University (05/30/25)
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  • Supervisor-Analytical Science

    Cambrex High Point (Durham, NC)
    …to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing ... from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (06/24/25)
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  • Quality Control Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position ... will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain...JOB RESPONSIBILITIES: + Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within… more
    Glenmark Pharmaceuticals Inc., USA (05/15/25)
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  • Analytical Data Reviewer

    Actalent (East Windsor, NJ)
    …clarity, and compliance in all documentation. + Maintain up-to-date copies of all cGMP documents in the laboratory and relevant databases. + Ensure all ... efforts, and contribute to continuous improvement initiatives within the laboratory . Responsibilities + Write, edit, and maintain Standard Operating Procedures… more
    Actalent (07/31/25)
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  • Sr. Director Quality Operations

    Fujifilm (College Station, TX)
    …Overview** The Senior Director Quality Operations is responsible for QA oversight of CGMP manufacturing operations and areas at one of our manufacturing ... equipment including but not limited to safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt), cleanroom (ISO… more
    Fujifilm (05/08/25)
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  • Microbiology Supervisor

    Actalent (Bowling Green, OH)
    …and compliance. Additional responsibilities include the preparation and maintenance of laboratory materials and equipment. Responsibilities + Ensure compliance with ... cGMP , GLP, and applicable standards. + Adhere to all...samples, and finished products. + Perform environmental monitoring of manufacturing areas, cleanrooms, and utilities. + Recommend and implement… more
    Actalent (07/27/25)
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